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Lavage and Suction of the Right Upper Quadrant to Reduce Post Laparoscopic Shoulder Pain

Lavage and Suction of the Right Upper Quadrant to Reduce Post Laparoscopic Shoulder Pain: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02004470
Enrollment
100
Registered
2013-12-09
Start date
2014-01-31
Completion date
2014-06-30
Last updated
2014-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder Pain

Keywords

post laparoscopic shoulder pain, active suction, lavage and suction, right shoulder pain, post operative shoulder pain

Brief summary

The use of laparoscopy in gynecologic surgery has been well established to decrease morbidity, blood loss, hospital stay, and post-operative pain when compared to traditional open abdominal surgery. However, the laparoscopic technique is associated with post-operative shoulder pain. We hypothesize that a combination of intraperitoneal saline lavage and active suction removal of carbon dioxide gas from the right upper quadrant of the abdomen will decrease incidence of post-laparoscopic shoulder pain when compared to passive exsufflation of carbon dioxide gas.

Interventions

PROCEDUREActive lavage and suction

Active lavage and suction of the right upper quadrant will be performed as the laparoscopic procedure is about to be terminated.

Sponsors

University of Tennessee
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* English speaking patient * Female * Age 18-75 * must undergo laparoscopic surgery * willing to participate in the study

Exclusion criteria

* Male patients * Under 18 or older than 75 * Laparoscopic procedures that get converted to laparotomy * Intraoperative hemorrhage more than 500 cc * Patients with active joint disease * History of shoulder surgery * Intraoperative laceration to the liver * Malignancy * Long term daily narcotic use * Chronic right upper quadrant/ shoulder pain * Pregnancy * History of dementia, Alzheimers, stroke or other condition causing altered mental status

Design outcomes

Primary

MeasureTime frameDescription
Pain Score12 hoursWe will assess pain scores based on visual analog score from 1-10 at 12 hours postoperatively.

Secondary

MeasureTime frameDescription
operative time24 hoursWe will assess how long each surgery takes to complete.
blood loss6 hoursWe will assess intraoperative blood loss.
analgesic use7 daysWe will assess total analgesic, iv and oral used over the course of 7 days postoperatively.
Anti emetic use48 hoursTotal amount of intravenous and oral narcotic used postoperatively.

Countries

United States

Contacts

Primary ContactMaryam Hadiashar, MD
maryamhad@gmail.com4086051927

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026